@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP984821.RAi3T5iISYBJeVK82rpNsVuVPphn-Skzw_BbBP-uMPha0> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP984821.RAi3T5iISYBJeVK82rpNsVuVPphn-Skzw_BbBP-uMPha0130_head {
  this: np:hasAssertion dgn-np:NP984821.RAi3T5iISYBJeVK82rpNsVuVPphn-Skzw_BbBP-uMPha0130_assertion;
    np:hasProvenance dgn-np:NP984821.RAi3T5iISYBJeVK82rpNsVuVPphn-Skzw_BbBP-uMPha0130_provenance;
    np:hasPublicationInfo dgn-np:NP984821.RAi3T5iISYBJeVK82rpNsVuVPphn-Skzw_BbBP-uMPha0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP984821.RAi3T5iISYBJeVK82rpNsVuVPphn-Skzw_BbBP-uMPha0130_assertion a np:Assertion .
  
  dgn-np:NP984821.RAi3T5iISYBJeVK82rpNsVuVPphn-Skzw_BbBP-uMPha0130_provenance a np:Provenance .
  
  dgn-np:NP984821.RAi3T5iISYBJeVK82rpNsVuVPphn-Skzw_BbBP-uMPha0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP984821.RAi3T5iISYBJeVK82rpNsVuVPphn-Skzw_BbBP-uMPha0130_assertion {
  miriam-gene:317773 a ncit:C16612 .
  
  lld:C1832884 a ncit:C7057 .
  
  dgn-gda:DGNcb5248f044008160d2b2595d0cf387ee sio:SIO_000628 miriam-gene:317773, lld:C1832884;
    a sio:SIO_001121 .
}

dgn-np:NP984821.RAi3T5iISYBJeVK82rpNsVuVPphn-Skzw_BbBP-uMPha0130_provenance {
  dgn-np:NP984821.RAi3T5iISYBJeVK82rpNsVuVPphn-Skzw_BbBP-uMPha0130_assertion dcterms:description
      "[These findings are consistent with the hypothesis that FHM mutations share the ability of rendering the brain more susceptible to CSD by causing either excessive synaptic glutamate release (FHM1) or decreased removal of K+ and glutamate from the synaptic cleft (FHM2) or excessive extracellular K+ (FHM3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:17395138;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP984821.RAi3T5iISYBJeVK82rpNsVuVPphn-Skzw_BbBP-uMPha0130_publicationInfo {
  this: dcterms:created "2015-08-25T14:47:42+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetv3.0rdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}